Skip to content
FDA.report
Public FDA data
NDC
RxNorm
DailyMed
Applications
GUDID
GMDN
PMA
PMN
MAUDE
Recalls
Search FDA.report
Search
Home
Company-Registration
1277005089
Device Listing 1277005089
Listing Summary
#
Listing key
1277005089
Premarket submission
K871763
Device
NEFA STANDARD SOLUTION CALIBRATOR
Applicant
Wako Chemicals USA, Inc.
Product code
JIT
Decision date
1987-05-26
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
232819
3005625991
3005625991
FUJIFILM Healthcare Americas Corporation
1
N
2026-01-01
1100 King Georges Post Rd Edison NJ US 08837